An American National Standard

Designation: D 93 02a

Designation: 34/99

Standard Test Methods for

Flash Point by Pensky-Martens Closed Cup Tester1

This standard is issued under the fixed designation D 93; the number immediately following the designation indicates the year of original
adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A superscript
epsilon (e) indicates an editorial change since the last revision or reapproval.
This standard has been approved for use by agencies of the Department of Defense.

INTRODUCTION

This flash point test method is a dynamic test method and depends on definite rates of temperature
increases to control the precision of the test method. The rate of heating may not in all cases give the
precision quoted in the test method because of the low thermal conductivity of certain materials. To
improve the prediction of flammability, Test Method D 3941, an equilibrium method, was developed
in which the heating rate is slower. This allows the vapor above the test specimen and the test
specimen to be at about the same temperature. If your specification requires Test Method D 93, do not
substitute Test Method D 3941 or any other test method without obtaining comparative data and
agreement from the specifier.
Flash point values are a function of the apparatus design, the condition of the apparatus used, and
the operational procedure carried out. Flash point can therefore only be defined in terms of a standard
test method, and no general valid correlation can be guaranteed between results obtained by different
test methods, or with test apparatus different from that specified.
1.4 These test methods is applicable for the detection of
contamination of relatively nonvolatile or nonflammable materials with volatile or flammable materials.
1.5 The values stated in SI units shall be regarded as the
standard. The values given in parentheses are provided for
information only.
1.6 This standard does not purport to address all of the
safety concerns, if any, associated with its use. It is the
responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. For specific hazards
statements, see 6.4, 7.1, 9.3, 9.4, 11.1.2, 11.1.4, and 12.1.2.

1. Scope *
1.1 These test methods cover the determination of the flash
point of petroleum products in the temperature range from 40
to 360C by a manual Pensky-Martens closed-cup apparatus or
an automated Pensky-Martens closed-cup apparatus.
NOTE 1Flash point determination as above 250C can be performed,
however, the precisions have not been determined above this temperature.
For residual fuels, precisions have not been determined for flash points
above 100C.

1.2 Procedure A is applicable to distillate fuels (diesel,

kerosine, heating oil, turbine fuels), new lubricating oils, and
other homogeneous petroleum liquids not included in the scope
of Procedure B.
1.3 Procedure B is applicable to residual fuel oils, cutback
residua, used lubricating oils, mixtures of petroleum liquids
with solids, petroleum liquids that tend to form a surface film
under test conditions, or are petroleum liquids of such kinematic viscosity that they are not uniformly heated under the
stirring and heating conditions of Procedure A.

2. Referenced Documents
2.1 ASTM Standards:
D 56 Test Methods for Flash Point by Tag Closed Cup
Tester2
D 3941 Test Method for Flash Point by the Equilibrium
Method with a Closed-Cup Apparatus3
D 4057 Practice for Manual Sampling for Petroleum and
Petroleum Products4

1
These test methods are under the joint jurisdiction of ASTM Committee D02 on
Petroleum Products and Lubricants and are the direct responsibility of Subcommittee D02.08 on Volatility. In the IP, these test methods are under the jurisdiction of
the Standardization Committee.
Current edition approved Dec. 10, 2002. Published March 2003. Originally
approved in 1921. Last previous edition approved in 2002 as D 9302.

Annual Book of ASTM Standards, Vol 05.01.

Annual Book of ASTM Standards, Vol 06.01.
4
Annual Book of ASTM Standards, Vol 05.02.
3

*A Summary of Changes section appears at the end of this standard.

Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.

D 93 02a
5. Significance and Use
5.1 The flash point temperature is one measure of the
tendency of the test specimen to form a flammable mixture
with air under controlled laboratory conditions. It is only one
of a number of properties which must be considered in
assessing the overall flammability hazard of a material.
5.2 Flash point is used in shipping and safety regulations to
define flammable and combustible materials. One should consult the particular regulation involved for precise definitions of
these classifications.

D 4177 Practice for Automatic Sampling of Petroleum and

Petroleum Products4
E 1 Specification for ASTM Thermometers5
E 300 Practice for Sampling Industrial Chemicals6
E 502 Test Method for Selection and Use of ASTM Standards for the Determination of Flash Point of Chemicals by
Closed Cup Methods7
2.2 ISO Standards8
Guide 34 Quality Systems Guidelines for the Production of
Reference Materials
Guide 35 Certification of Reference MaterialGeneral and
Statistical Principles

NOTE 2The U.S. Department of Transportation (DOT)9 and U.S.

Department of Labor (OSHA) have established that liquids with a flash
point under 37.8C (100F) are flammable, as determined by these test
methods, for those liquids which have a kinematic viscosity of 5.8 mm 2/s
(cSt) or more at 37.8C or 9.5 mm 2/s (cSt) or more at 25C (77F), or that
contain suspended solids, or have a tendency to form a surface film while
under test. Other classification flash points have been established by these
departments for liquids using these test methods.

3. Terminology
3.1 Definitions:
3.1.1 dynamic, adjin petroleum productsthe condition
where the vapor above the test specimen and the test specimen
are not in temperature equilibrium at the time that the ignition
source is applied.
3.1.1.1 DiscussionThis is primarily caused by the heating
of the test specimen at the constant prescribed rate with the
vapor temperature lagging behind the test specimen temperature.
3.1.2 equilibrium, nin petroleum productsthe condition
where the vapor above the test specimen and the test specimen
are at the same temperature at the time the ignition source is
applied.
3.1.2.1 DiscussionThis condition may not be fully
achieved in practice, since the temperature may not be uniform
throughout the test specimen, and the test cover and shutter on
the apparatus can be cooler.
3.1.3 flash point, nin petroleum products, the lowest
temperature corrected to a barometric pressure of 101.3 kPa
(760 mm Hg), at which application of an ignition source causes
the vapors of a specimen of the sample to ignite under specified
conditions of test.
3.1.3.1 DiscussionThe test specimen is deemed to have
flashed when a flame appears and instantaneously propagates
itself over the entire surface of the test specimen.
3.1.3.2 DiscussionWhen the ignition source is a test
flame, the application of the test flame may cause a blue halo
or an enlarged flame prior to the actual flash point. This is not
a flash point and shall be ignored.

5.3 These test methods should be used to measure and

describe the properties of materials, products, or assemblies in
response to heat and an ignition source under controlled
laboratory conditions and should not be used to describe or
appraise the fire hazard or fire risk of materials, products, or
assemblies under actual fire conditions. However, results of
these test methods may be used as elements of a fire risk
assessment which takes into account all of the factors which
are pertinent to an assessment of the fire hazard of a particular
end use.
5.4 These test methods provides the only closed cup flash
point test procedures for temperatures up to 370C (698F).
6. Apparatus
6.1 Pensky-Martens Closed Cup Apparatus (manual)This
apparatus consists of the test cup, test cover and shutter,
stirring device, heating source, ignition source device, air bath,
and top plate described in detail in Annex A1. The assembled
manual apparatus, test cup, test cup cover, and test cup
assembly are illustrated in Figs. A1.1-A1.4, respectively. Dimensions are listed respectively.
6.2 Pensky-Martens Closed Cup Apparatus (automated)
This apparatus is an automated flash point instrument that is
capable of performing the test in accordance with Section 11
(Procedure A) and Section 12 (Procedure B) of these test
methods. The apparatus shall use the test cup, test cover and
shutter, stirring device, heating source, and ignition source
device described in detail in Annex A1.
6.3 Temperature Measuring DeviceIs a thermometer having a range as shown as follows and conforming to the
requirements prescribed in Specification E 1 or in Annex A3, or
an electronic temperature measuring device, such as resistance
thermometers or thermocouples. The device shall exhibit the
same temperature response as the mercury thermometers.

4. Summary of Test Method

4.1 A brass test cup of specified dimensions, filled to the
inside mark with test specimen and fitted with a cover of
specified dimensions, is heated and the specimen stirred at
specified rates, by either of two defined procedures (A or B).
An ignition source is directed into the test cup at regular
intervals with simultaneous interruption of the stirring, until a
flash is detected (see 3.1.3.1). The flash point is reported as
defined in 3.1.3.
5

9
For information on U.S. Department of Transportation regulations, see Codes
of U.S. Regulations 49 CFR Chapter 1 and the U.S. Department of Labor, see 29
CFR Chapter XVII. Each of these items is revised annually and may be procured
from the Superintendent of Documents, Government Printing Office, Washington,
DC 20402.

Annual Book of ASTM Standards, Vol 14.03.

Annual Book of ASTM Standards, Vol 15.05.
7
Annual Book of ASTM Standards, Vol 14.02.
8
Available from American National Standards Institute (ANSI), 25 W. 43rd St.,
4th Floor, New York, NY 10036.
6

D 93 02a
Temperature Range
5 to +110C (20 to 230F)
+10 to 200C (50 to 392F)
+90 to 370C (200 to 700F)

before transferring to the specimen cup. No sample shall be

heated and transferred unless its temperatures is more than
18C or 32F below its expected flash point. When the sample
has been heated above this temperature, allow the sample to
cool until its temperature is at least 18C or 32F below the
expected flash point before transferring.

Thermometer Number
ASTM
IP
9C (9F)
15C
88C (88F)
101C
10C (10F)
16C

6.4 Ignition SourceNatural gas flame, bottled gas flame,

and electric ignitors (hot wire) have been found acceptable for
use as the ignition source. The gas flame device described in
detailed in Fig. A1.4 requires the use of the pilot flame
described in A1.1.2.3. The electric ignitors shall be of the
hot-wire type and shall position the heated section of the
ignitor in the aperture of the test cover in the same manner as
the gas flame device. (WarningGas pressure supplied to the
apparatus should not be allowed to exceed 3 kPa (12 in.) of
water pressure.)

NOTE 3Volatile vapors can escape during heating when the sample
container is not properly sealed.
NOTE 4Some viscous samples may not completely liquefy even after
prolonged periods of heating. Care should be exercised when increasing
the heating temperature to avoid unnecessary loss of volatile vapors, or
heating the sample too close to the flash point.

8.7 Samples containing dissolved or free water may be

dehydrated with calcium chloride or by filtering through a
qualitative filter paper or a loose plug of dry absorbent cotton.
Warming the sample is permitted, but it shall not be heated for
prolonged periods or greater than a temperature of 18C 32F
below its expected flash point.

7. Reagents and Materials

7.1 Cleaning SolventsUse suitable solvent capable of
cleaning out the specimen from the test cup and drying the test
cup and cover. Some commonly used solvents are toluene and
acetone. (WarningToluene, acetone, and many solvents are
flammable and a health hazard. Dispose of solvents and waste
material in accordance with local regulations.)

NOTE 5If the sample is suspected of containing volatile contaminants,

the treatment described in 8.6 and 8.7 should be omitted.

9. Preparation of Apparatus
9.1 Support the manual or automated apparatus on a level
steady surface, such as a table.
9.2 Tests are to be performed in a draft-free room or
compartment. Tests made in a laboratory hood or in any
location where drafts occur are not reliable.

8. Sampling
8.1 Obtain a sample in accordance with instructions given in
Practices D 4057, D 4177, or E 300.
8.2 At least 75 mL of sample is required for each test. Refer
to Practice D 4057. When obtaining a sample of residual fuel
oil, the sample container shall be from 85 to 95 % full. For
other types of samples, the size of the container shall be chosen
such that the container is not more than 85 % full or less than
50 % full prior to any sample aliquot being taken.
8.3 Successive test specimens can be taken from the same
sample container. Repeat tests have been shown to be within
the precisions of the method when the second specimen is
taken with the sample container at least 50 % filled. The results
of flash point determinations can be affected if the sample
volume is less than 50 % of sample container capacity.
8.4 Erroneously high flash points may be obtained if precautions are not taken to avoid the loss of volatile material. Do
not open containers unnecessarily, to prevent loss of volatile
material or possible introduction of moisture, or both. Avoid
storage of samples at temperatures in excess of 35C or 95F.
Samples for storage shall be capped tightly with inner seals. Do
not make a transfer unless the sample temperature is at least the
equivalent of 18C or 32F below the expected flash point.
8.5 Do not store samples in gas-permeable containers, since
volatile material may diffuse through the walls of the enclosure. Samples in leaky containers are suspect and not a source
of valid results.
8.6 Samples of very viscous materials shall be heated in
their containers, with lid/cap slightly loosened to avoid buildup
of dangerous pressure, at the lowest temperature adequate to
liquefy any solids, not exceeding 28C or 50F below the
expected flash point, for 30 min. If the sample is then not
completely liquefied, extend the heating period for additional
30 min periods as necessary. Then gently agitate the sample to
provide mixing, such as orbiting the container horizontally,

NOTE 6A shield, of the approximate dimensions 460 mm (18 in.)

square and 610 mm (24 in.) high, or other suitable dimensions, and having
an open front is recommended to prevent drafts from disturbing the vapors
above the test cup.
NOTE 7With some samples whose vapors or products of pyrolysis are
objectionable, it is permissible to place the apparatus along with a draft
shield in a ventilation hood, the draft of which is adjustable so that vapors
can be withdrawn without causing air currents over the test cup during the
ignition source application period.

9.3 Prepare the manual apparatus or the automated apparatus for operation in accordance with the manufacturers instructions for calibrating, checking, and operating the equipment. (WarningGas pressure should not be allowed to
exceed 3 kPa (12 in.) of water pressure.)
9.4 Thoroughly clean and dry all parts of the test cup and its
accessories before starting the test, to ensure the removal of
any solvent which had been used to clean the apparatus. Use
suitable solvent capable of removing all of the specimen from
the test cup and drying the test cup and cover. Some commonly
used solvents are toluene and acetone. (WarningToluene,
acetone, and many solvents are flammable. Health hazard.
Dispose of solvents and waste material in accordance with
local regulations.)
10. Verification of Apparatus
10.1 Adjust the automated flash point detection system
(when used) in accordance with the manufacturers instructions.
10.2 Verify that the temperature measuring device is in
accordance with 6.3.
10.3 Verify the performance of the manual apparatus or the
automated apparatus at least once per year by determining the
3

D 93 02a
11.1.4 Turn the stirring device at 90 to 120 rpm, stirring in
a downward direction. (WarningMeticulous attention to all
details relating to the ignition source, size of test flame or
intensity of the electric ignitor, rate of temperature increase,
and rate of dipping the ignition source into the vapor of the test
specimen is desirable for good results.)
11.1.5 Application of Ignition Source:
11.1.5.1 If the test specimen is expected to have a flash point
of 110C or 230F or below, apply the ignition source when the
temperature of the test specimen is 23 6 5C or 41 6 9F
below the expected flash point and each time thereafter at a
temperature reading that is a multiple of 1C or 2F. Discontinue the stirring of the test specimen and apply the ignition
source by operating the mechanism on the test cover which
controls the shutter so that the ignition source is lowered into
the vapor space of the test cup in 0.5 s, left in its lowered
position for 1 s, and quickly raised to its upward position.
11.1.5.2 If the test specimen is expected to have a flash point
above 110C or 230F, apply the ignition source in the manner
described in 11.1.5.1 at each temperature increase of 2C or
5F, beginning at a temperature of 23 6 5C or 41 6 9F
below the expected flash point.
11.1.6 When testing materials to determine if volatile material contamination is present, it is not necessary to adhere to
the temperature limits for initial ignition source application as
stated in 11.1.5.
11.1.7 When testing materials where the expected flash
point temperature is not known, bring the material to be tested
and the tester to a temperature of 15 6 5C or 60 6 10F.
When the material is known to be very viscous at this
temperature, heat the specimen to a starting temperature as
described in 8.6. Apply the ignition source, in the manner
described in 11.1.5.1, beginning at least 5C or 10F higher
than the starting temperature.

flash point of a certified reference material (CRM) such as

those listed in Annex A4, which is reasonably close to the
expected temperature range of the samples to be tested. The
material shall be tested according to Procedure A of these test
methods and the observed flash point obtained in 11.1.8 or
11.2.2 shall be corrected for barometric pressure (see Section
13). The flash point obtained shall be within the limits stated in
Table A4.1 for the identified CRM or within the limits
calculated for an unlisted CRM (see Annex A4).
10.4 Once the performance of the apparatus has been
verified, the flash point of secondary working standards
(SWSs) can be determined along with their control limits.
These secondary materials can then be utilized for more
frequent performance checks (see Annex A4).
10.5 When the flash point obtained is not within the limits
stated in 10.3 or 10.4, check the condition and operation of the
apparatus to ensure conformity with the details listed in Annex
A1, especially with regard to tightness of the lid (A1.1.2.2), the
action of the shutter, the position of the ignition source
(A1.1.2.3), and the angle and position of the temperature
measuring device (A1.1.2.4). After any adjustment, repeat the
test in 10.3 using a fresh test specimen, with special attention
to the procedural details prescribed in these test methods.
PROCEDURE A
11. Procedure
11.1 Manual Apparatus:
11.1.1 Ensure that the sample container is filled to the
volume capacity requirement specified in 8.2. Fill the test cup
with the test specimen to the filling mark inside of the test cup.
The temperature of the test cup and test specimen shall be at
least 18C or 32F below the expected flash point. If too much
test specimen has been added to the test cup, remove the excess
using a syringe or similar device for withdrawal of fluid. Place
the test cover on the test cup and place the assembly into the
apparatus. Be sure the locating or locking device is properly
engaged. If the temperature measuring device is not already in
place, insert the device into its holder.
11.1.2 Light the test flame, and adjust it to a diameter of 3.2
to 4.8 mm (0.126 to 0.189 in.), or switch on the electric igniter
and adjust the intensity in accordance with the manufacturers
instructions. (WarningGas pressure should not be allowed
to exceed 3 kPa (12 in.) of water pressure.) (Warning
Exercise care when using a gas test flame. If it should be
extinguished it will not ignite the vapors in the test cup, and the
gas for the test flame that then enters the vapor space can
influence the result.) (WarningThe operator should exercise
and take appropriate safety precautions during the initial
application of the ignition source, since test specimens containing low-flash material can give an abnormally strong flash
when the ignition source is first applied.) (WarningThe
operator should exercise and take appropriate safety precautions during the performance of these test methods. The
temperatures attained during these test methods, up to 370C
(698F), are considered hazardous.)
11.1.3 Apply the heat at such a rate that the temperature, as
indicated by the temperature measuring device, increases 5 to
6C (9 to 11F)/min.

NOTE 8Flash Point results determined in an unknown expected flash

point mode should be considered approximate. This value can be used as
the expected flash point when a fresh specimen is tested in the standard
mode of operation.

11.1.8 Record as the observed flash point the reading on the

temperature measuring device at the time ignition source
application causes a distinct flash in the interior of the test cup.
The sample is deemed to have flashed when a large flame
appears and instantaneously propagates itself over the entire
surface of the test specimen. (WarningFor certain mixtures
containing halogenated hydrocarbons, such as, methylene chloride or trichloroethylene, no distinct flash, as defined, is
observed. Instead a significant enlargement of the test flame
(not halo effect) and change in color of the test flame from blue
to yellowish-orange occurs. Continued heating and testing of
these samples above ambient temperature can result in significant burning of vapors outside the test cup, and can be a
potential fire hazard. See Appendix X1 and Appendix X2 for
more information.)
11.1.9 When the ignition source is a test flame, the application of the test flame may cause a blue halo or an enlarged
flame prior to the actual flash point. This is not a flash and shall
be ignored.
4

D 93 02a
and take appropriate safety precautions during the initial
application of the ignition source, since test specimens containing low-flash material may give an abnormally strong flash
when the ignition source is first applied.) (WarningThe
operator should exercise and take appropriate safety precautions during the performance of these test methods. The
temperatures attained during these test methods, up to 370C
(698F), are considered hazardous.)
12.1.3 Turn the stirring device at 250 6 10 rpm, stirring in
a downward direction.
12.1.4 Apply the heat at such a rate that the temperature as
indicated by the temperature measuring device increases 1 to
1.6C (2 to 3F)/min.
12.1.5 Proceed as prescribed in Section 11, with the exception of the preceding requirements for rates of stirring and
heating.
12.2 Automated Apparatus:
12.2.1 The automated apparatus shall be capable of performing the procedure as described in 12.1, including control
of the heating rate, stirring of the test specimen, application of
the ignition source, detection of the flash point, and recording
the flash point.
12.2.2 Start the automated apparatus in accordance with the
manufacturers instructions. The apparatus shall follow the
procedural details in accordance with 12.1.3 through 12.1.5.

11.1.10 When a flash point is detected on the first application, the test shall be discontinued, the result discarded, and the
test repeated with a fresh test specimen. The first application of
the ignition source with the fresh test specimen shall be 23 6
5C or 41 6 9F below the temperature at which a flash point
was detected on the first application.
11.1.11 When a flash point is detected at a temperature
which is greater than 28C or 50F above the temperature of
the first application of the ignition source, or when a flash point
is detected at a temperature which is less than 18C or 32F
above the temperature of the first application of the ignition
source, the result shall be considered approximate, and the test
repeated with a fresh test specimen. Adjust the expected flash
point for this next test to the temperature of the approximate
result. The first application of the ignition source with the fresh
test specimen shall be 23 6 5C or 416 9F below the
temperature at which the approximate result was found.
11.1.12 When the apparatus has cooled down to a safe
handling temperature, less than 55C (130F), remove the test
cover and the test cup and clean the apparatus as recommended
by the manufacturer.
NOTE 9Exercise care when cleaning and positioning the lid assembly
so not to damage or dislocate the flash detection system or temperature
measuring device. See the manufacturers instructions for proper care and
maintenance.

11.2 Automated Apparatus:

11.2.1 The automated apparatus shall be capable of performing the procedure as described in 11.1, including control
of the heating rate, stirring of the test specimen, application of
the ignition source, detection of the flash point, and recording
the flash point.
11.2.2 Start the automated apparatus in accordance with the
manufacturers instructions. The apparatus shall follow the
procedural details described in 11.1.3 through 11.1.8.

PRECISION, CALCULATION, AND REPORT FOR

PROCEDURES A AND B
13. Calculation
13.1 Observe and record the ambient barometric pressure
(see Note 10) at the time of the test. When the pressure differs
from 101.3 kPa (760 mm Hg), correct the flash point as
follows:

PROCEDURE B
12. Procedure
12.1 Manual Apparatus:
12.1.1 Ensure that the sample container is filled to the
volume capacity requirement specified in 8.2. Fill the test cup
with the test specimen to the filling mark inside of the test cup.
The temperature of the test cup and test specimen shall be at
least 18C or 32F below the expected flash point. If too much
test specimen has been added to the test cup, remove the excess
using a syringe or similar device for withdrawal of fluid. Place
the test cover on the test cup and place the assembly into the
apparatus. Be sure the locating or locking device is properly
engaged. If the temperature measuring device is not already in
place, insert the device into its holder.
12.1.2 Light the test flame and adjust it to a diameter of 3.2
to 4.8 mm (0.126 to 0.189 in.), or switch on the electric igniter
and adjust the intensity in accordance with the manufacturers
instructions. (WarningGas pressure should not be allowed
to exceed 3 kPa (12 in.) of water pressure.) (Warning
Exercise care when using a gas test flame. If it should be
extinguished it will not ignite the vapors in the test cup and the
gas for the test flame that then enters the vapor space can
influence the result.) (WarningThe operator should exercise

Corrected flash point 5 C 1 0.25 ~101.3 K!

(1)

Corrected flash point 5 F 1 0.06 ~760 P!

(2)

Corrected flash point 5 C 1 0.033 ~760 P!

(3)

where:
C = observed flash point, C,
F = observed flash point, F,
P = ambient barometric pressure, mm Hg, and
K = ambient barometric pressure, kPa.
NOTE 10The barometric pressure used in this calculation is the
ambient pressure for the laboratory at the time of the test. Many aneroid
barometers, such as those used at weather stations and airports, are
precorrected to give sea level readings and would not give the correct
reading for this test.

13.2 After correction for barometric pressure, round the

temperature to the nearest 0.5C (1F) and record.
14. Report
14.1 Report the corrected flash point as the ASTM D 93IP
34, Procedure A or Procedure B Pensky-Martens Closed Cup
Flash Point of the test specimen.
5

D 93 02a
manual apparatus and 21 laboratories participated with the
automated equipment) and a 1994 IP cooperative test program
using 12 fuel samples and 4 pure chemicals. (Twenty-six
laboratories participated with manual and automated equipment. The apparatus used either a gas test flame or an electric
resistance (hot wire) device for the ignition source. Information
on the type of samples and their average flash point are in the
research report.10

15. Precision and Bias (Procedure A)

15.1 PrecisionThe precision of this procedure as determined by the statistical examination of the interlaboratory test
results, is as follows:
15.1.1 RepeatabilityThe difference between successive
results, obtained by the same operator with the same apparatus
under constant operating conditions on identical test material,
would in the long run, in the normal and correct operation of
the test method, exceed the following values in 1 case in 20.
r 5 AX,

16. Precision and Bias (Procedure B)

16.1 PrecisionThe precision of this procedure as determined by the statistical examination of the interlaboratory test
results, is as follows:
16.1.1 RepeatabilityThe difference between successive
results obtained by the same operator with the same apparatus
under constant operating conditions on identical test materials
would, in the long run, in the normal and correct operation of
the test method, exceed the following value in 1 case in 20:

(4)

A 5 0.029,
X 5 mean result in C, and
r 5 repeatability.

15.1.2 ReproducibilityThe difference between two single

and independent results, obtained by different operators working in different laboratories on identical material, would in the
long run, in the normal and correct operation of the test
method, exceed the following values only in 1 case in 20.
R 5 BX,

Residual fuel oil 2C ~5F!

Other types 5C ~9F!

(5)

(6)

16.1.2 ReproducibilityThe difference between two single

and independent results obtained by different operators working in different laboratories on identical material would, in the
long run, exceed the following value only in 1 case in 20.

B 5 0.071,
X 5 mean result in C, and
R 5 reproducibility.

Residual fuel oil 6C ~12F!

Other types 10C ~18F!

15.1.3 BiasSince there is no accepted reference material

suitable for determining the bias for the procedure in these test
methods, bias has not been determined.
15.1.4 Relative BiasStatistical evaluation of the data did
not detect any significant difference between the reproducibility variances of manual and automated Pensky-Martens flash
point results for the samples studied. Evaluation of the data did
not detect any significant difference between averages of
manual and automated Pensky-Martens flash point for the
samples studied with the exception of cycle oil and fuel oil
which showed some bias. In any case of dispute, the manual
procedure shall be considered the referee test.

(7)

16.1.3 BiasSince there is no accepted reference material

suitable for determining the bias for the procedure in these test
methods, bias has not been determined.
16.1.4 The precision data for residual fuel oils were developed in a 1996 cooperative test program conducted by the IP
using 12 samples of residual fuel and 40 laboratories worldwide using both the manual and automated apparatus. Information on the type of samples and their average flash point are
in the research report.
16.1.5 The precision data for other sample types in Procedure B is not known to have been developed in accordance
with RR:D021007.11

NOTE 11The precision statements were derived on clear liquids only.

Refer to the research report10 for information regarding relative bias and
types of samples. Additional studies are in progress concerning relative
bias.

NOTE 12Procedure B was not tested in the 1991 interlaboratory

program.

15.1.5 The precision data were developed from a combined

1991 ASTM cooperative test program10 using 5 samples of fuel
and lubricating oils (Twelve laboratories participated with the

17. Keywords
17.1 automated flash point; automated Pensky-Martens
closed cup; flammability; flash point; Pensky-Martens closed
cup

10
Supporting data (the results of the 1991 interlaboratory cooperative test
program) have been filed at ASTM International Headquarters and may be obtained
by requesting Research Report RR: S151008.

11
Supporting data have been filed at ASTM International Headquarters and may
be obtained by requesting Research Report RR: D021007.

D 93 02a
ANNEXES
(Mandatory Information)
A1. APPARATUS SPECIFICATIONS

A1.1 A typical assembly of the apparatus, gas heated, is

shown in Fig. A1.1. The apparatus shall consist of a test cup,
cover, and stove conforming to the following requirements:

A1.1.1 CupThe cup shall be of brass, or other nonrusting

metal of equivalent heat conductivity, and shall conform to the
dimensional requirements in Fig. A1.2. The flange shall be

NOTE 1Lid assembly can be positioned either right or left-handed.

FIG. A1.1 Pensky-Martens Closed Flash Tester

D 93 02a

mm

mm

A
B
C
D
E
F
G
H
I
J

D
E
F
G
H
I
J
K
L

(in.)

min

max

(min)

(max)

79.0
1.0
2.8
21.72
45.47
50.72
55.75
3.8
53.90
2.29

79.8
...
3.6
21.84
45.72
50.85
56.00
4.0
54.02
2.54

(3.11)
(0.04)
(0.11)
(0.855)
(1.790)
(1.997)
(2.195)
(0.15)
(2.122)
(0.090)

(3.14)
(...)
(0.14)
(0.860)
(1.800)
(2.002)
(2.205)
(0.16)
(2.127)
(0.100)

(in.)

min

max

(min)

(max)

12.7
4.8
13.5
23.8
1.2
7.9
12.00
16.38
18.65

13.5
5.6
14.3
24.6
2.0
...
12.32
17.00
19.45

(0.50)
(0.19)
(0.53)
(0.94)
(0.05)
(0.31)
(0.472)
(0.645)
(0.734)

(0.53)
(0.22)
(0.56)
(0.97)
(0.08)
(...)
(0.485)
(0.669)
(0.766)

FIG. A1.3 Cover Proper

openings A, B, and C in the cover are completely closed, and

when in the other extreme position, these openings are completely opened. The mechanism operating the shutter should be
of the spring type and constructed so that when at rest the
shutter shall exactly close the three openings. When operated
to the other extreme, the three cover openings shall be exactly
open and the tip of the exposure tube shall be fully depressed.
A1.1.2.3 Flame-Ignition DeviceThe flame-ignition device (Fig. A1.4) shall have a tip with an opening 0.69 to 0.79
mm (0.027 to 0.031 in.) in diameter. This tip shall be made
preferably of stainless steel, although it may be fabricated of
other suitable metals. The flame-exposure device shall be
equipped with an operating mechanism which, when the
shutter is in the open position, depresses the tip so that the
center of the orifice is between the planes of the under and
upper surfaces of the cover proper at a point on a radius passing
through the center of the larger opening A (Fig. A1.3). An
electric ignitor is also suitable. The electric ignitors shall be of
the electric resistance (hot-wire) type and shall position the
heated section of the ignitor in the aperture of the test cover in
the same manner as the gas flame device.
A1.1.2.4 Pilot FlameA pilot flame shall be provided for
automatic relighting of the exposure flame. A bead 4 mm
(532 in.) in diameter can be mounted on the cover so that the

FIG. A1.2 Test Cup

equipped with devices for locating the position of the cup in the
stove. A handle attached to the flange of the cup is a desirable
accessory. The handle shall not be so heavy as to tip over the
empty cup.
A1.1.2 Cover:
A1.1.2.1 Cover ProperThe cover shown in Fig. A1.3
shall be of brass (A1.1.1) and shall have a rim projecting
downward almost to the flange of the cup. The rim shall fit the
outside of the cup with a clearance not exceeding 0.36 mm
(0.014 in.) on the diameter. There shall be a locating or locking
device, or both, engaging with a corresponding device on the
cup. The four openings in the cover, A, B, C, and D, are shown
in Fig. A1.3. The upper edge of the cup shall be in close contact
with the inner face of the cover throughout its circumference.
A1.1.2.2 ShutterThe cover shall be equipped with a brass
shutter (Fig. A1.1 and Fig. A1.4), approximately 2.4 mm (332
in.) thick, operating on the plane of the upper surface of the
cover. The shutter shall be so shaped and mounted that it
rotates on the axis of the horizontal center of the cover between
two stops, so placed, that when in one extreme position, the
8

D 93 02a

mm

A
B
C
D
E
F
G
H
IA
J
K
L
M
N
A

(in.)

min

max

(min)

(max)

18.3
2.38
7.6
2.0
0.69
2.0
6.4
9.6
43.0
50.0
...
1.22
31.8
7.6

19.8
3.18
8.4
2.8
0.79
2.8
10.4
11.2
46.0
51.6
0.36
2.06
44.4
8.4

(0.72)
(0.094)
(0.30)
(0.08)
(0.027)
(0.08)
(0.25)
(0.38)
(1.69)
(1.97)
(...)
(0.048)
(1.25)
(0.30)

(0.78)
(0.125)
(0.33)
(0.11)
(0.031)
(0.11)
(0.41)
(0.44)
(1.81)
(2.03)
(0.014)
(0.08)
(1.75)
(0.33)

Includes tolerance for length of thermometer given in Specification E 1.

FIG. A1.4 Test Cup and Cover Assembly

size of the test flame can be regulated by comparison. The tip

of the pilot flame shall have an opening the same size as the tip
of the flame exposure device (0.69 to 0.79 mm (0.027 to 0.031
in.) in diameter).
A1.1.2.5 Stirring DeviceThe cover shall be equipped with
a stirring device (Fig. A1.4) mounted in the center of the cover
and carrying two 2-bladed metal propellers. In Fig. A1.4 lower
propeller is designated by the letters L, M, and N. This

propeller shall measure approximately 38 mm from tip to tip,

with each of its two blades 8 mm in width with a pitch of 45.
The upper propeller is designated by the letters A, C, and G.
This propeller measures approximately 19 mm, tip to tip, each
of its two blades is also 8 mm in width with a pitch of 45. Both
propellers are located on the stirrer shaft in such a manner that,
when viewed from the bottom of the stirrer, the blades of one
propeller are at 0 and 180 while the blades of the other

D 93 02a
6.4 mm (14 in.) in thickness unless the heating element is
designed to give equal heat flux densities over all the wall and
bottom surfaces.
A1.1.2.9 Heater, Electric ResistanceIf the heater is of the
electric resistance type, it shall be constructed so that all parts
of the interior surface are heated uniformly. The wall and
bottom of the air bath shall not be less than 6.4 mm (14 in.) in
thickness unless the resistance heating elements are distributed
over at least 80 % of the wall and all the bottom of the air bath.
A heater having such a distribution of the heating elements
positioned at least 4.0 mm (532 in.) away from the internal
surface of the heating unit can be used in conjunction with a
minimum thickness of 1.58 mm (116 in.) for the wall and
bottom of the air bath.
A1.1.2.10 Top PlateThe top plate shall be of metal, and
shall be mounted with an air gap between it and the air bath. It
may be attached to the air bath by means of three screws and
spacing bushings. The bushings should be of proper thickness
to define an air gap of 4.8 mm (316 in.), and they shall be not
more than 9.5 mm (38 in.) in diameter.

propeller are at 90 and 270. A stirrer shaft may be coupled to

the motor by a flexible shaft or a suitable arrangement of
pulleys.
A1.1.2.6 StoveHeat shall be supplied to the cup by means
of a properly designed stove which is equivalent to an air bath.
The stove shall consist of an air bath and a top plate on which
the flange of the cup rests.
A1.1.2.7 Air BathThe air bath shall have a cylindrical
interior and shall conform to the dimensional requirements in
Fig. A1.1. The air bath may be either a flame or electrically
heated metal casting (A1.1.2.8), or an electric-resistance element (A1.1.2.9). In either case, the air bath must be suitable for
use at the temperatures to which it will be subjected without
deformation.
A1.1.2.8 Heater, Flame or ElectricIf the heating element
is a flame or an electric heater, it shall be so designed and used
that the temperatures of the bottom and the walls are approximately the same. In order that the air bath internal surfaces
should be at a uniform temperature, it should not be less than

A2. MANUFACTURING STANDARDIZATION OF THERMOMETER AND FERRULE

A2.1 The low-range thermometer, which conforms also to

the specification for the cup thermometer in the tag closed
tester (Test Method D 56) and which frequently is fitted with a
metal ferrule intended to fit the collar on the cover of the tag
flash tester, can be supplemented by an adapter (Fig. A2.1) to
be used in the larger diameter collar of the Pensky-Martens
apparatus. Differences in dimensions of these collars, which do

not affect test results, are a source of unnecessary trouble to

manufacturers and suppliers of instruments, as well as to users.
A2.2 Dimensional requirements are shown in Fig. A2.1.
Conformity to these requirements is not mandatory, but is
desirable to users as well as suppliers of Pensky-Martens
testers.

10

D 93 02a

mm

A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P

(in.)

min

max

(min)

(max)

6.20
17.0
9.80
11.92
1.40
8.56
12.4
8.56
8.1
9.9
8.64
5.1
17.0
27.4
7.11
9.73

6.50
18.0
9.85
12.24
1.65
8.61
13.0
8.61
8.6
10.7
8.69
5.6
17.5
28.2
7.16
9.78

(0.244)
(0.67)
(0.386)
(0.469)
(0.055)
(0.337)
(0.49)
(0.337)
(0.32)
(0.39)
(0.340)
(0.20)
(0.67)
(1.08)
(0.280)
(0.383)

(0.256)
(0.71)
(0.388)
(0.482)
(0.065)
(0.339)
(0.57)
(0.339)
(0.34)
(0.42)
(0.342)
(0.22)
(0.69)
(1.11)
(0.282)
(0.385)

FIG. A2.1 Dimensions for Thermometer Adapter, Ferrule, and Packing Ring

A3. THERMOMETER SPECIFICATIONS

A3.1 See Fig. A3.1 and Tables A3.1-A3.4.

11

D 93 02a

FIG. A3.1 Test Gage for Checking Enlargements on Thermometers

TABLE A3.1 IP Thermometer Specifications

NOTEThe stem shall be made with an enlargement having a diameter of 1.5 to 2.0 mm greater than the stem and a length of 3 to 5 mm, the bottom
of the enlargement being 64 to 66 mm from the bottom of the bulb. These dimensions shall be measured with the test gage shown in Fig. A3.1.
IP 15C

IP 16C

IP 101C

Pensky-Martens Low

Pensky-Martens High

Pensky-Martens Medium

Name
Range
Graduation
Immersion, mm
Overall length 65 mm
Stem diameter, mm
Bulb shape
Bulb length, mm
Bulb diameter, mm

Length of graduated portion,

mm
Distance bottom of bulb to,
mm
Longer lines at each
Figured at each
Expansion chamber
Top finish
Scale error not to exceed 6
See notes

5 to + 110C
0.5C
57
290
6.0 to 7.0
cylindrical
9 to 13
not less than 5.5 and
not greater than
stem
140 to 175

90 to 370C
2C
57
280 6 10
6.0 to 7.0
cylindrical
7 to 10
not less than 4.5 and
not greater than
stem
143 to 180

20 to 150C
1C
57
290
6.0 to 7.0
cylindrical
9 to 13
not less than 5.5 and
not greater than
stem
140 to 175

0C
85 to 95
1 and 5C
5C
required
ring
0.5C

90C
80 to 90
10 and 20C
20C
required
ring
1 to 260C
2C above 260C
1 and Table A3.2 for
emergent stem
temperatures

20C
85 to 95
5C
5C
required
ring
1C

1 and Table A3.2 for

emergent stem
temperatures

12

1 and Table A3.2 for

emergent stem
temperatures

5 to

13

For
Test
at

57

57

Immersion

10C

25F

5F

5F

1C

2C

1F

0.5C

Subdivisions

Long
Lines
at
Each

50F

20C

10F

5C

Number
at
Each

IMM

ASTM
10C or
10F
57 mm

320F

9C or
9F
57 mm
IMM

ASTM 160C

Special
Inscription Permit
Heating to

1F

0.5C

Scale
Error,
max

Expansion
Chamber

287

287

Total
Length
65

6.0
to
7.0

7.0

to

6.0

Stem
OD

8.0
to
10.0

13

to

9.0

Length

OD

4.5
to
6.0

not
greater
than
stem

Bulb

230F

110C

32F

0C

Bottom
of
Bulb
to
Line
at

86
to
99

98

to

85

Distance

680F

360C

212F

100C

Bottom
of
Bulb
to
Line
at

Scale Location

227
to
245

237

to

221

DisRange
tance

Bottom
of
Bulb
to
Ice
Point

Ice Point
Scale

Distance
to
Bottom,
min

7.5
to
8.5

8.5

to

7.5

2.5
to
5.0A

5.0

to

2.5

Length

64
to
66

66

to

64

Distance
to
Bottom

Stem Enlargement

Distance
to
OD
Top,
max

Contraction
Chamber

The length of the enlargement, and the distance from the bottom of the enlargement to the bottom of the bulb shall be measured with the test gage shown in Fig. A3.1.
Scale error: 1C up to 260C; 2C over 260C.
C
An expansion chamber is provided for relief of gas pressure to avoid distortion of the bulb at higher temperatures. It is not for the purpose of joining mercury separations; and under no circumstances should the
thermometer be heated above the highest temperature reading.
D
Scale error: 2.5F up to 500F; 3.5F over 500F.

10C-62 90 to
Pensky- 370C
Martens,
High- (200 to
Range
10F-62 700F)

Martens
LowRange
Tag
(20 to
Closed
Tester 230F)
9F-62

Pensky- +110C

9C-62

ASTM
Number
Range
and
Name

Graduations

TABLE A3.2 Specifications for ASTM Thermometers

All dimensions are in millimetres.
See Table A3.3 for Standardization Temperature.

D 93 02a

D 93 02a
TABLE A3.3 Standardization Temperatures

NOTEThe emergent column temperatures are those attained when using the thermometers in the test equipment for which the thermometers were
originally designed. In some cases these temperatures are markedly different from those realized during standardization.
Temperature

Average
Temperature of
Emergent
Column

Temperature

Average
Temperature of
Emergent
Column

Average
Temperature of
Emergent
Column

Temperature

Temperature

Thermometer 9C
(5 to + 100C)
0C
19C
35C
28C
70C
40C
105C
50C

Thermometer 9F
(20 to 230F)
32F
66F
100F
86F
160F
106F
220F
123F

Thermometer 10C
(90 to 370C)
100C
61C
200C
71C
300C
87C
370C
104C

Thermometer 10F
(200 to 700F)
212F
141F
390F
159F
570F
180F
700F
220F

IP 15C (7 to 110C)
0C
19C
20C
20C
40C
31C
70C
40C
100C
48C

IP 15F (20 to 230F)

32F
66F
70F
70F
100F
86F
150F
104F
212F
118F

IP 16C (90 to 370C)

100C
61C
150C
65C
200C
71C
250C
78C
300C
87C
350C
99C

IP 16F (20 to 700F)

200F
140F
300F
149F
400F
160F
500F
175F
600F
195F
700F
220F

TABLE A3.4 Specifications for Medium-Range Pensky-Martens

ASTM No. 88F (88C) Vegetable Oil Flash Thermometer
Name
Reference Fig. No.
Range
For test at
A
Immersion, mm
Graduations:
Subdivisions
Long lines at each
Numbers at each
Scale error, max
Special inscription

B
C
D
E

F
G

H
I
J
K
L
M
A

Average
Temperature of
Emergent
Column

Expansion chamber:
Permit heating to
Total length, mm
Stem OD, mm
Bulb length, mm
Bulb OD, mm
Scale location:
Bottom of bulb to line at
Distance, mm
Length of graduated portion, mm
Ice-point scale:
Range
Bottom of bulb to ice-point, mm
Contraction chamber:
Distance to bottom, min, mm
Distance to top, max, mm
Stem enlargement:
OD, mm
Length, mm
Distance to bottom, mm

Medium-Range Pensky-Martens
5
50392F

10200C

57
0.5C
1C and 5C
5C
0.5C

1F
5F
10F
1F
ASTM
88F (88C)
57 mm IMM

205C

400F
285 to 295
6.0 to 7.0
8.0 to 12.0
>4.5 and <stemA

20C

68F
80 to 90
145 to 180

7.5 to 8.5
2.5 to 5.0A
64 to 66

Bulb OD shall be greater than 4.5 mm and less than the outside diameter of the stem (C).

14

D 93 02a

A4. VERIFICATION OF APPARATUS PERFORMANCE

will provide certificates stating the method-specific flash point

for each material of the current production batch. Calculation
of the limits for these other CRMs can be determined from the
reproducibility value of these test methods, reduced by interlaboratory effect and then multiplied by 0.7. See Research
Report RR:S15-1008.10

A4.1 Certified Reference Material (CRM)CRM is a

stable, pure (99 + mole % purity) hydrocarbon or other stable
petroleum product with a method-specific flash point established by a method-specific interlaboratory study following
ASTM RR:D02-1007 guidelines11 or ISO Guide 34 and 35.
A4.1.1 Values of the flash point corrected for barometric
pressure for some reference materials and their typical limits
are given in Table A4.112 (see Note A4.1). Suppliers of CRMs

NOTE A4.1Materials, purities, flash point values, and limits stated in

Table A4.1 were developed in an ASTM interlaboratory program to
determine suitability of use for verification fluids in flash point test
methods. Other materials, purities, flash point values, and limits can be
suitable when produced according to the practices of ASTM RR:D021007 or ISO Guides 34 and 35. Certificates of performance of such
materials should be consulted before use, as the flashpoint value will vary
dependent on the composition of each CRM batch.

TABLE A4.1 D 93 Typical Flash Point Values and Typical Limits

for CRM

NOTESupporting data for the interlaboratory study to generate the

flash point in Table A4.1 can be found in research report RR:S15-1010.12
Hydrocarbon

ndecane
nundecane
ntetradecane
nhexadecane

Purity, mole %

Flash Point,C

Limits, C

99 +
99 +
99 +
99 +

52.8
68.7
109.3
133.9

62.3
63.0
64.8
65.9

A4.2 Secondary Working Standard (SWS)SWS is a

stable, pure (99 + mole % purity) hydrocarbon, or other petroleum product whose composition is known to remain appreciably stable.
A4.2.1 Establish the mean flash point and the statistical
control limits (3s) for the SWS using standard statistical
techniques. (See ASTM MNL 7).13

12
Supporting data have been filed at ASTM International Headquarters and may
be obtained by requesting Research Report RR: S151010.

13
Manual on Presentation of Data and Control Chart Analysis, ASTM MNL, 6th
ed., ASTM International, W. Conshohocken, 1990.

APPENDIXES
(Nonmandatory Information)
X1. FLASH POINT MASKING PHENOMENON

X1.1 A condition during flash point testing can occur with

certain mixtures whereby the nonflammable component of the
sample tends to inert the vapor space above the liquid, thus
preventing a flash. Under this condition, the flash point of the
material is masked resulting in the reporting of incorrect high
flash point or no flash point.

test flame from blue to yellow-orange laminar flame is observed.

X1.4 Under this condition, continued heating and testing
for flash point at temperatures above ambient temperature,
have resulted in significant burning of the ignitable vapor
outside the test cup, often above the test flame. This can be a
potential fire hazard if not recognized.

X1.2 This flash point masking phenomenon most frequently occurs with ignitable liquids that contain certain
halogenated hydrocarbons such as dichloromethane (methylene chloride) and trichloroethylene.

X1.5 It is recommended that if this condition is encountered during the flash point testing of these type of materials,
testing should be discontinued.

X1.3 Under this condition, no distinct flash as defined in

3.1.3 of these test methods is observed. Instead a significant
enlargement of the test flame and a change in the color of the

X1.6 Further commentaries regarding flash point test and

flammability of mixtures can be found in Test Method E 502.

15

D 93 02a
X2. FLASH POINT TEST AND FLAMMABILITY OF MIXTURES

X2.1 While the flash point can be used to indicate the

flammability of liquid materials for certain end uses, flash point
does not represent the minimum temperature at which a
material can evolve flammable vapors.

components, there are cases where this liquid can evolve

flammable vapors under certain conditions and yet will not
exhibit a close-cup flash point. This phenomenon is noted
when a nonflammable component is sufficiently volatile and
present in sufficient quantity to inert the vapor space of the
closed cup, thus preventing a flash. In addition, there are
certain instances where an appreciable quantity of the nonflammable component will be present in the vapor, and the material
will exhibit no flash point.

X2.2 There are instances with pure materials where the

absence of a flash point does not ensure freedom from
flammability. Included in this category are materials that
require large diameters for flash propagation, such as trichloroethylene. This material will not propagate a flame in apparatus the size of a flash point tester, however, its vapors are
flammable and will burn when ignited in apparatus of adequate
size.

X2.4 Liquids containing a highly volatile nonflammable

component or impurity, which exhibit no flash point because of
the influence of the nonflammable material, may form flammable mixtures if totally flash vaporized in air in the proper
proportions.

X2.3 When a liquid contains flammable and nonflammable

SUMMARY OF CHANGES
Subcommittee D02.08 has identified the location of selected changes to this standard since the last issue
(D 9302) that may impact the use of this standard.
(1) Added a paragraph to the Introduction about flash point
values being dependent on the test procedure used.

(2) Deleted Note 2 and renumbered the notes.

ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentioned
in this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the risk
of infringement of such rights, are entirely their own responsibility.
This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years and
if not revised, either reapproved or withdrawn. Your comments are invited either for revision of this standard or for additional standards
and should be addressed to ASTM International Headquarters. Your comments will receive careful consideration at a meeting of the
responsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you should
make your views known to the ASTM Committee on Standards, at the address shown below.
This standard is copyrighted by ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959,
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address or at 610-832-9585 (phone), 610-832-9555 (fax), or service@astm.org (e-mail); or through the ASTM website
(www.astm.org).

16